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评估头孢地尔克罗在与复杂临床分离株进行测试时的药敏纸片扩散法与肉汤微量稀释法结果。

Assessment of cefiderocol disk diffusion versus broth microdilution results when tested against complex clinical isolates.

机构信息

Institute of Antibiotics, Huashan Hospital, Fudan University , Shanghai, China.

Department of Clinical Laboratory, The First Affiliated Hospital of Nanchang University , Nanchang, China.

出版信息

Microbiol Spectr. 2023 Dec 12;11(6):e0535522. doi: 10.1128/spectrum.05355-22. Epub 2023 Oct 19.

Abstract

Carbapenem-resistant is a major global health concern due to its high prevalence and limited treatment options. Cefiderocol is the only novel Food and Drug Administration (FDA)-approved β-lactam agent for the salvage treatment of carbapenem-resistant infection. Currently, a commercial automated susceptibility testing panel of cefiderocol is unavailable. Both the preparation of iron-depleted cation-adjusted Mueller-Hinton broth and the performance of broth microdilution are cumbersome in routine microbiology laboratories. A disk diffusion method is convenient for cefiderocol antimicrobial susceptibility testing, but limited data are available specifically for clinical isolates. Moreover, the Clinical and Laboratory Standards Institute published revisions to the cefiderocol disk diffusion breakpoints in 2022. Hence, we evaluated the performance of cefiderocol disk diffusion compared with the reference BMD against clinical isolates, especially those with cefiderocol zone diameters ≤ 14 mm.

摘要

碳青霉烯类耐药性是一个全球性的主要健康问题,因为其高患病率和有限的治疗选择。头孢他啶/阿维巴坦是唯一一种新型的美国食品和药物管理局(FDA)批准的用于治疗碳青霉烯类耐药性感染的β-内酰胺类药物。目前,商业上可获得的头孢他啶/阿维巴坦自动药敏检测板尚不可用。铁耗竭阳离子调整 Mueller-Hinton 肉汤的制备和肉汤微量稀释的操作在常规微生物学实验室中都很繁琐。纸片扩散法方便用于头孢他啶/阿维巴坦药敏检测,但针对 临床分离株的数据有限。此外,临床和实验室标准研究所(CLSI)于 2022 年修订了头孢他啶/阿维巴坦纸片扩散的折点。因此,我们评估了头孢他啶/阿维巴坦纸片扩散法与参考 BMD 对 临床分离株的性能比较,特别是那些头孢他啶/阿维巴坦抑菌环直径≤14mm 的分离株。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f1ae/10714814/daaed2f92de5/spectrum.05355-22.f001.jpg

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